510(k) K132147

Device
2D PERFUSION
Applicant
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
510(k) number
K132147
Product code
OWB  
Decision
Substantially Equivalent (SESE)
Decision date
2013-12-16
Date received
2013-07-11
Regulation
892.1650
Classification name
Interventional Fluoroscopic X-ray System
Medical specialty
Radiology
Review panel
Radiology
Device class
2
Clearance type
Abbreviated
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
LISELOTTE KORNMANN
Address
Veenpluis 4-6 Best Noord-Brabant NL 5684 pc 5684 pc

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

Other 510(k) Records For Product Code OWB  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
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K252503Intelligent NRCanon, Inc.2026-04-30
K254173ARTIS icono floor; ARTIS icono biplane; ARTIS icono ceiling; ARTIS phenoSiemens Medical Solutions USA, Inc.2026-04-24
K253752ARTIS genio floor; ARTIS icono.explore floorSiemens Medical Solutions USA, Inc.2026-04-23
K252229BELLIGER ACEGenoray Co., Ltd.2026-04-02
K252099TriniasShimadzu Corporation2026-03-24
K253584Alphenix, INFX-8000V/B, INFX-8000V/S, V9.6 with aEvolve Imaging (FOV Extension)Canon Medical Systems Corporation2026-03-10
K252500CARA SystemCara Medical, Ltd.2026-02-20
K251992ArmSure Fluoroscopic Positioning SystemSavfe Co. , Ltd.2026-02-11
K254186Azurion R3.1Philips Medical Systems B.V.2026-01-16
K252068MC2 Portable X-ray SystemOxos Medical2025-12-22
K251893SKAN C PULSARSkanray Technologies Limited2025-12-16
K251199Allia MoveoGE Medical Systems SCS2025-12-09
K250241Cios SelectSiemens Medical Solutions USA, Inc.2025-11-04
K251827Azurion R3.1Philips Medical Systems B.V.2025-10-24

Legacy Summary#

summary

FDA Review#

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